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B4930

Sigma-Aldrich

Capillary Electrophoresis Running Buffer (10x)

for automated DNA sequencing

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Synonym(s):
Running Buffer, Sequencing Buffer
NACRES:
NA.25

grade

for molecular biology

Quality Level

200

type

for automated DNA sequencing

form

liquid

technique(s)

DNA sequencing: suitable

storage temp.

room temp

Application

Capillary Electrophoresis Running Buffer (10x) has been used for automated sequencing by capillary electrophoresis.

Features and Benefits

  • Compatible with ABI Prism 3700 DNA Analyzer and Molecular Dynamics MegaBACE capillary electrophoresis instruments
  • Provides consistency and high performance for every batch
  • Stable at room temperature for convenient shipping, and storage
  • Tested and works well with the performance-optimized polymer 6 (POP6)
  • Cost-efficient - high-quality buffer at a great value
  • Quality control testing of every lot ensures proper pH, conductivity, and performance for Capillary Electrophoresis Sequencing
  • Plastic bottles provide easy handling
  • Available in one, four and 20 L as well as custom packaging options available

Preparation Note

Product should be diluted to 1x before use. Add 1 volume of the 10X capillary electrophoresis buffer solution to 9 volumes of deionized water. Cover the top of the container and mix the 1X solution by inversion.

Other Notes

Capillary Electrophoresis Buffer is for laboratory use only. Not for drug, household, or other uses.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H290 - H314

Hazard Classifications

Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible, corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

监管及禁止进口产品

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Wolf-Matthias Leeder et al.
Bio-protocol, 11(5), e3935-e3935 (2021-04-03)
Gene expression within the mitochondria of African trypanosomes and other protozoan organisms relies on a nucleotide-specific RNA-editing reaction. In the process exclusively uridine (U)-nucleotides are site-specifically inserted into and deleted from sequence-deficient primary transcripts to convert them into translatable mRNAs.

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